Variant Details

Variant: esv3623926

Internal ID

7010782

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr10:79745548..79842753	hg38	UCSC Ensembl
	chr10:81505304..81602509	hg19	UCSC Ensembl

Cytoband

10q22.3

Allele length

Assembly	Allele length
hg38	97206
hg19	97206

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv13870228, essv13870211, essv13870207, essv13870244, essv13870210, essv13870259, essv13870225, essv13870233, essv13870262, essv13870242, essv13870234, essv13870235, essv13870229, essv13870215, essv13870256, essv13870236, essv13870239, essv13870217, essv13870245, essv13870251, essv13870222, essv13870212, essv13870218, essv13870209, essv13870230, essv13870237, essv13870250, essv13870223, essv13870227, essv13870253, essv13870258, essv13870241, essv13870255, essv13870261, essv13870248, essv13870208, essv13870238, essv13870232, essv13870240, essv13870220, essv13870224, essv13870254, essv13870246, essv13870221, essv13870219, essv13870214, essv13870252, essv13870226, essv13870216, essv13870213, essv13870243, essv13870260, essv13870231, essv13870247, essv13870249, essv13870257

Samples

HG01795, HG01443, NA19399, HG01188, HG00457, HG02323, NA19057, NA21137, HG03139, HG02384, HG00654, NA18526, HG01503, NA18550, HG00589, HG01488, NA18993, HG02561, HG02389, HG03045, HG01176, HG00705, HG00637, HG01709, NA18638, HG00675, HG01524, HG02136, HG00982, HG02397, HG02449, NA18871, HG00551, HG02537, HG00692, NA20876, NA19064, HG03021, NA18946, HG01182, HG01842, HG01865, HG01812, NA18632, HG03866, HG02089, HG00285, HG02501, HG00631, HG02401, HG00381, HG02079, HG01846, HG01600, HG01807, NA20585

Known Genes

LOC642361

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3623926

Frequency

Sample Size	2504
Observed Gain	56
Observed Loss	0
Observed Complex	0
Frequency	n/a